Paul D. Rubin is a corporate partner based in the Washington, D.C. office and is the Co-Chair of the firm’s Healthcare & Life Sciences Group and the Chair of the FDA Regulatory practice. His practice focuses on FDA/FTC regulatory matters. Mr. Rubin has been recognized as a leading practitioner by Chambers USA for Regulatory Healthcare and The Legal 500 US for Life Sciences and Advertising and Marketing Litigation. He has been ranked as an LMG Life Sciences Star by LMG Life Sciences every year since the editorial was first published in 2013 and was recently a finalist for LMG Life Sciences’ “Regulatory Attorney of the Year.” (2019)
Mr. Rubin represents FDA-regulated drug, device and consumer product companies on a wide range of issues ranging from strategic regulatory counseling to complex compliance and enforcement matters. He also routinely conducts regulatory due diligence for private equity funds and strategic acquirers in corporate transactions.
In addition to his FDA practice, Mr. Rubin also has substantial experience helping clients navigate complex advertising/promotion and privacy-related issues, including FTC investigations, negotiating FTC settlements/consent decrees, disputes before the National Advertising Division of the Better Business Bureau (NAD) and advertising lawsuits under Section 43(a) of the Lanham Act. Mr. Rubin also has considerable experience advising consumer product companies on CPSC-related compliance, including Section 15(b) submissions and “Fast Track Recalls.”
Mr. Rubin is a contributing author to the Health Care Mergers and Acquisitions Answer Book (Practising Law Institute, 2019) and the co-author of various articles, including “Infringing Influencers? Federal Judge Says Sponsored Blogger Can Face Trademark Infringement Liability,” IP Watchdog (August, 2021); “Lessons From Federal Fraud Charges Against UBiome,” Law360 (April, 2021); “The American Rescue Plan Act of 2021: Pharmaceutical Industry Impact,” Pharm Exec (March, 2021); “Destruction Emerges as a Powerful Enforcement Measure for AI: FTC Requires Company to Delete Models Trained with Improperly Utilized Consumer Data,” Compliance & Enforcement (January, 2021); “Debevoise & Plimpton Discusses State Marijuana Initiatives and Financial Institutions,” Columbia Blue Sky Blog (November, 2020); “Trump's Drug Pricing Order Is More Bark Than Bite,” Law360 (September, 2020); “Providers, Investors Need Clear Post-Covid Telehealth Picture,” Bloomberg Law (September, 2020); “Expert Analysis: COVID-19 Raises Unique Issues For Health, Life Sciences Cos.,” Law360 (March, 2020); “Insight: The SEC/FDA Nexus: Best Practices for Publicly Traded Life Sciences Companies,” Bloomberg Law (November, 2019); “Expert Analysis: Drugmaker Fine Shows SEC's Renewed Disclosure Focus,” Law360 (August, 2019); “How Life Sciences Cos. Can Prepare for Legal and PR Crises,” Law360 (December, 2018); “A Look at Recent Efforts to Contain Health Care Costs,” Law360 (January, 2018); and “How Tax Reform Could Impact the Health Care Industry,” Law360 (November, 2017). He is also a frequent lecturer on FDA/FTC law and has guest lectured at the University of Pennsylvania Law School.
Mr. Rubin joined Debevoise in 2017. He earned his J.D. cum laude from the University of Pennsylvania Law School in 1992. He received a B.S. in Economics magna cum laude from the University of Pennsylvania Wharton School of Business in 1989.